A citation-based method for searching scientific literature

Rita Genesio, Giuseppe Maria Maruotti, Gabriele Saccone, Angela Mormile, Anna Conti, Rita Cicatiello, Viviana Sarnataro, Angelo Sirico, Antonella Izzo, Pasquale Martinelli, Lucio Nitsch. Clin Case Rep 2018
Times Cited: 2







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


GALNT14 mediates tumor invasion and migration in breast cancer cell MCF-7.
Tian Huanna, Zuo Tao, Wang Xiangfei, An Longfei, Xie Yuanyuan, Wang Jianhua, Zhang Cuifang, Jiao Manjing, Cao Wenjing, Qin Shaochuan,[...]. Mol Carcinog 2015
42
50

Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities.
Gabriel C Dworschak, Markus Draaken, Alina C Hilger, Charlotte Schramm, Enrika Bartels, Eberhard Schmiedeke, Sabine Grasshoff-Derr, Stefanie Märzheuser, Stefan Holland-Cunz, Martin Lacher,[...]. Birth Defects Res A Clin Mol Teratol 2015
13
50



Malrotation and volvulus in infancy and childhood.
A J W Millar, H Rode, S Cywes. Semin Pediatr Surg 2003
56
50

GALNT14 genotype as a response predictor for concurrent chemoradiotherapy in advanced esophageal squamous cell carcinoma.
Yung-Kuan Tsou, Kung-Hao Liang, Wey-Ran Lin, Hsien-Kun Chang, Chen-Kan Tseng, Chau-Ting Yeh. Oncotarget 2017
9
50

Familial malrotation: report of three affected siblings.
S Beaudoin, A Mathiot-Gavarin, G Gouizi, F Bargy. Pediatr Surg Int 2005
4
50

Intestinal malrotation: the role of small intestinal dysmotility in the cause of persistent symptoms.
R C Coombs, R G Buick, P G Gornall, J J Corkery, I W Booth. J Pediatr Surg 1991
16
50

Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome.
Anna Lindstrand, Erica E Davis, Claudia M B Carvalho, Davut Pehlivan, Jason R Willer, I-Chun Tsai, Subhadra Ramanathan, Craig Zuppan, Aniko Sabo, Donna Muzny,[...]. Am J Hum Genet 2014
53
50

No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations.
Johanna Winberg, Håkan Berggren, Torsten Malm, Sune Johansson, Jens Johansson Ramgren, Boris Nilsson, Agne Liedén, Agneta Nordenskjöld, Peter Gustavsson, Ann Nordgren. Eur J Med Genet 2015
4
50

Expanding the phenotype of alveolar capillary dysplasia (ACD).
Partha Sen, Nivedita Thakur, David W Stockton, Claire Langston, Bassem A Bejjani. J Pediatr 2004
88
50

Cilia in vertebrate left-right patterning.
Agnik Dasgupta, Jeffrey D Amack. Philos Trans R Soc Lond B Biol Sci 2016
40
50

Jack Barney Award. The changing spectrum of intestinal malrotation: diagnosis and management.
Marcene R McVay, Evan R Kokoska, Richard J Jackson, Samuel D Smith. Am J Surg 2007
39
50


Integration of left-right Pitx2 transcription and Wnt signaling drives asymmetric gut morphogenesis via Daam2.
Ian C Welsh, Michael Thomsen, David W Gludish, Catalina Alfonso-Parra, Yan Bai, James F Martin, Natasza A Kurpios. Dev Cell 2013
44
50

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.
Trilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, Allen N Lamb, J Britt Ravnan, Roger A Schultz, Beth S Torchia, Nicholas Neill, Ian Casci, Bassem A Bejjani,[...]. Genet Med 2011
70
50

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, Jenneke van den Ende, Edwin Reyniers, Marco Fichera, Corrado Romano, Barbara Delle Chiaie, Geert Mortier, Björn Menten,[...]. Eur J Med Genet 2009
113
50

Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish.
Wolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, Miriam Armenio, Jesper Eisfeldt, Nikos Papadogiannakis, Peter Gustavsson, Anna Lindstrand. Hum Mutat 2018
7
50

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
Paweł Stankiewicz, Partha Sen, Samarth S Bhatt, Mekayla Storer, Zhilian Xia, Bassem A Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J Driscoll, Melissa K Maisenbacher,[...]. Am J Hum Genet 2009
259
50

Congenital intestinal malrotation in adolescent and adult patients: a 12-year clinical and radiological survey.
Britt Husberg, Karin Salehi, Trevor Peters, Ulf Gunnarsson, Margareta Michanek, Agneta Nordenskjöld, Karin Strigård. Springerplus 2016
18
50

Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
Karin Salehi Karlslätt, Maria Pettersson, Nina Jäntti, Przemyslaw Szafranski, Tomas Wester, Britt Husberg, Ulla Ullberg, Pawel Stankiewicz, Ann Nordgren, Johanna Lundin,[...]. Mol Genet Genomic Med 2019
6
50


Identification of GALNT14 as a novel neuroblastoma predisposition gene.
Marilena De Mariano, Roberta Gallesio, Marco Chierici, Cesare Furlanello, Massimo Conte, Alberto Garaventa, Michela Croce, Silvano Ferrini, Gian Paolo Tonini, Luca Longo. Oncotarget 2015
25
50

The chirality of gut rotation derives from left-right asymmetric changes in the architecture of the dorsal mesentery.
Nicole M Davis, Natasza A Kurpios, Xiaoxia Sun, Jerome Gros, James F Martin, Clifford J Tabin. Dev Cell 2008
95
50

Intestinal malrotation needs immediate consideration and investigation.
Semire Serin Ezer, Pelin Oguzkurt, Abdulkerim Temiz, Emine Ince, Hasan Ozkan Gezer, Senay Demir, Akgun Hicsonmez. Pediatr Int 2016
3
50


The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
50

Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia.
Ellen A Tsai, Christopher M Grochowski, Alexandra M Falsey, Ramakrishnan Rajagopalan, Danielle Wendel, Marcella Devoto, Ian D Krantz, Kathleen M Loomes, Nancy B Spinner. Hum Mutat 2015
25
50

Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome.
Agne Liedén, Malin Kvarnung, Daniel Nilssson, Ellika Sahlin, Elisabeth Syk Lundberg. Am J Med Genet A 2014
25
50


Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways.
Maria Pettersson, Heli Viljakainen, Petra Loid, Taina Mustila, Minna Pekkinen, Miriam Armenio, Johanna C Andersson-Assarsson, Outi Mäkitie, Anna Lindstrand. J Clin Endocrinol Metab 2017
17
50

Review of genetic factors in intestinal malrotation.
Vicki Martin, Charles Shaw-Smith. Pediatr Surg Int 2010
42
50

Persistent gastrointestinal symptoms after correction of malrotation.
S P Devane, R Coombes, V V Smith, W M Bisset, I W Booth, B D Lake, P J Milla. Arch Dis Child 1992
28
50


GALNT14 Genotype Predicts Postoperative Outcome of Stage III Colorectal Cancer With Oxaliplatin as Adjuvant Chemotherapy.
Wey-Ran Lin, Jy-Ming Chiang, Kung-Hao Liang, Siew-Na Lim, Ming-Wei Lai, Yung-Kuan Tsou, Tzu-Yun Hsieh, Chih-Kai Hsu, Chau-Ting Yeh. Medicine (Baltimore) 2016
10
50

Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite.
Avinash V Dharmadhikari, Tomasz Gambin, Przemyslaw Szafranski, Wenjian Cao, Frank J Probst, Weihong Jin, Ping Fang, Krzysztof Gogolewski, Anna Gambin, Jaya K George-Abraham,[...]. BMC Med Genet 2014
9
50

Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.
J D Cody, P D Ghidoni, B R DuPont, D E Hale, S G Hilsenbeck, R F Stratton, D S Hoffman, S Muller, R L Schaub, R J Leach,[...]. Am J Med Genet 1999
93
50

Analysis of clinical variation seen in patients with 18q terminal deletions.
G Strathdee, E H Zackai, R Shapiro, J Kamholz, J Overhauser. Am J Med Genet 1995
79
50

Ciliopathy spectrum expanded? Jeune syndrome associated with foregut dysmotility and malrotation.
Tim Hall, Andrew Bush, John Fell, Amaka Offiah, Virpi Smith, Robin Abel. Pediatr Pulmonol 2009
5
50

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
50

Duplication and deletion of CFC1 associated with heterotaxy syndrome.
Ruixue Cao, Fei Long, Liping Wang, Yuejuan Xu, Ying Guo, Fen Li, Sun Chen, Kun Sun, Rang Xu. DNA Cell Biol 2015
3
50

7q11.23 Duplication syndrome: Physical characteristics and natural history.
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, Omar Abdul-Rahman, Sarah L Dugan, Alan F Rope, Patricia Bader, Laura G Hendon, Shelley L Velleman, Bonita P Klein-Tasman,[...]. Am J Med Genet A 2015
37
50

Familial midgut volvulus.
S L Smith. Surgery 1972
12
50

Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association.
Johanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, Ellika Sahlin, Frideborg Bradley, Edvard Nordenskjöld, Pär-Johan Svensson, Göran Annerén, Erik Iwarsson, Ann Nordgren,[...]. PLoS One 2014
20
50

Expanded conventional first trimester screening.
Jonathan B Carmichael, Hsiao-Pin Liu, David Janik, Terrence W Hallahan, Kypros H Nicolaides, David A Krantz. Prenat Diagn 2017
12
50

Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions.
Darío G Lupiáñez, Katerina Kraft, Verena Heinrich, Peter Krawitz, Francesco Brancati, Eva Klopocki, Denise Horn, Hülya Kayserili, John M Opitz, Renata Laxova,[...]. Cell 2015
896
50

Towards an evidence-based process for the clinical interpretation of copy number variation.
E R Riggs, D M Church, K Hanson, V L Horner, E B Kaminsky, R M Kuhn, K E Wain, E S Williams, S Aradhya, H M Kearney,[...]. Clin Genet 2012
60
50

Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
21
50


Relationship between nuchal translucency thickness and prevalence of major cardiac defects in fetuses with normal karyotype.
A Atzei, K Gajewska, I C Huggon, L Allan, K H Nicolaides. Ultrasound Obstet Gynecol 2005
82
50


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.